SCOPUS 정보 검색 플랫폼

Volumn 212, Issue 3, 2000, Pages 108-109

Hereditary fructose intolerance as cause of hepatomegaly with isolated increase in γGT in a 5 year old boy;Hereditare fruktoseintoleranz (HFI) als ursache einer isolierten γGT- erhohung bei einem 5-jahrigen jungen mit hepatomegalie

(4) Wossmann W a Wiemann, J a Korber F a Gortner, L a

a JUSTUS LIEBIG UNIVERSITY (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ECHOGRAPHY; FEEDING BEHAVIOR; HEPATOMEGALY; HEREDITARY FRUCTOSE INTOLERANCE; LIVER BIOPSY; NUTRITION; BIOPSY; BLOOD; CASE REPORT; DIFFERENTIAL DIAGNOSIS; ENZYMOLOGY; GENETICS; HETEROZYGOTE DETECTION; HUMAN; LIVER; MALE; MUTATION; PATHOLOGY; PRESCHOOL CHILD;

FRUCTOSE BISPHOSPHATE ALDOLASE; GAMMA GLUTAMYLTRANSFERASE;

BIOPSY; CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; FRUCTOSE INTOLERANCE; FRUCTOSE-BISPHOSPHATE ALDOLASE; GAMMA-GLUTAMYLTRANSFERASE; HEPATOMEGALY; HETEROZYGOTE DETECTION; HUMANS; LIVER; MALE; MUTATION;

EID: 0034184394 PISSN: 03008630 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (3)

References (7)

1
- 0031945356
- Hereditary fructose intolerance
- 1 Ali M, Rellos P, Cox TM. Hereditary fructose intolerance. J Med Genet 1998; 35: 353-365
- (1998) J Med Genet , vol.35 , pp. 353-365
- Ali, M.¹ Rellos, P.² Cox, T.M.³

2
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- Molecular analysis of aldolase B genes in hereditary fructose intolerance
- 2 Cross NCP, de Franchis R, Sebastio G, Dazzo C, Tolan DR, Gregori C, Odievre M. Vidailhet M, Romano V, Mascali G, Romano C, Musumeci S, Steinmann B, Glitzelmann R, Cox TM. Molecular analysis of aldolase B genes in hereditary fructose intolerance. Lancet 1998; 335: 306-309
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- Cross, N.C.P.¹ De Franchis, R.² Sebastio, G.³ Dazzo, C.⁴ Tolan, D.R.⁵ Gregori, C.⁶ Odievre, M.⁷ Vidailhet, M.⁸ Romano, V.⁹ Mascali, G.¹⁰ Romano, C.¹¹ Musumeci, S.¹² Steinmann, B.¹³ Glitzelmann, R.¹⁴ Cox, T.M.¹⁵

3
- 0025282839
- Molecular evidence for compound heterozygosity in hereditary fructose intolerance
- 3 Dazzo C, Tolan DR. Molecular evidence for compound heterozygosity in hereditary fructose intolerance. Am J Hum Gen 1990; 46: 1194-1199
- (1990) Am J Hum Gen , vol.46 , pp. 1194-1199
- Dazzo, C.¹ Tolan, D.R.²

4
- 0025304655
- Hereditary fructose intolerance in the vomiting infant
- 4 Edstrom CS. Hereditary fructose intolerance in the vomiting infant. Pediatrics 1990; 85: 600-603
- (1990) Pediatrics , vol.85 , pp. 600-603
- Edstrom, C.S.¹

5
- 0001662863
- Disorders of fructose metabolism
- Scriver CR, Beaudet AL, Sly WS, Valle D (Hrsg). New York: McGraw-Hill
- 5 Glitzelmann R, Steinmann B, van den Berge G. Disorders of fructose metabolism. In: Scriver CR, Beaudet AL, Sly WS, Valle D (Hrsg): Metabolic basis of inherited disease. New York: McGraw-Hill, 1995
- (1995) Metabolic Basis of Inherited Disease
- Glitzelmann, R.¹ Steinmann, B.² Van Den Berge, G.³

6
- 0029954183
- Neonatal screening for hereditary fructose intolerance: Frequency of the most common mutant aldolase B allele (A149P) in the British population
- 6 James CL, Rellos P, Ali M, Heeley AF, Cox TM. Neonatal screening for hereditary fructose intolerance: frequency of the most common mutant aldolase B allele (A149P) in the British population. J Med Genet 1996; 33: 837-841
- (1996) J Med Genet , vol.33 , pp. 837-841
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7
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- Screening for hereditary fructose intolerance by revers dot-blot
- 7 Lau J, Tolan DR. Screening for hereditary fructose intolerance by revers dot-blot. Mol Cell Probes 1999; 13: 35-40
- (1999) Mol Cell Probes , vol.13 , pp. 35-40
- Lau, J.¹ Tolan, D.R.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.